If you are the parent of a child with Epilepsy, there’s great opportunity for you to experience summer programs all around the country. How about camp?

For those of you around the world, if you’ve never participated in a gathering or fundraiser for your local Epilepsy Foundation, I highly suggest it! It’s very easy to do, and not only will your Epilepsy Foundation benefit, but you stand to gain so much!

A film done to honor Evan Moss and his life with Epilepsy, just won the top prize at the Neuro Film fest and the Fan Favorite Award.

For those of us, young and old, who live with Epilepsy, stress can be a huge contributor to seizures.

Meet an incredible Epilepsy advocate…a Mom who lost a child to Epilepsy.

So often, we all get wrapped up in communicating through social media outlets and spreading the word about Epilepsy via chatrooms. Are we caught up on the news about the disease?

My Grandma, despite her toughness, had a remarkable capacity for understanding Epilepsy…my Epilepsy.

Once you get the ‘NO’ on surgery and you’ve experimented with multiple meds, is there anything left that will help you take back your life from a life of seizures?

More than likely there is a drug-treatment out there for your Epilepsy, but it’s a matter of managing your expectations

We just returned from the National Walk for Epilepsy, held this past weekend in Washington DC. WHAT A DAY! I think it can sometimes be overwhelming and downright emotional, particularly for my tiny family, when you realize that thousands of people…many with Epilepsy, many supporting family-members who live with the disease, care enough to walk for this cause, and contribute much-needed funds.